ZMP

C19orf26 (2 of 2)

Ensembl ID:

ENSDARG00000089348

Description:

chromosome 19 open reading frame 26 [Source:HGNC Symbol;Acc:28617]

Human Orthologue:

C19orf26

Human Description:

chromosome 19 open reading frame 26 [Source:HGNC Symbol;Acc:28617]

Mouse Orthologue:

Dos

Mouse Description:

downstream of Stk11 Gene [Source:MGI Symbol;Acc:MGI:1354170]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18348	Nonsense	Available for shipment	Available now
sa19916	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa18348

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122394	Nonsense	188	631	3	3

Genomic Location (Zv9):

Chromosome 2 (position 59909389)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	58979818
GRCz11	2	59077109

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGGAGGCTGGAGCATCAGGAGGMGGTGGGGAGGAGTTTGKASCCATGGGT[C/T]AGTTGGARAGCCTGGATCAGCCCAGTCTGTACCGTGATATCTGGAGTCTG

Long Flanking Sequence:

TCTGTACTGTACAGCTCAGTTGAAATCTTTGGGTTTTAGAAAAGAAGGACTGGACACGTCTGCTCTAATTCTTGGCATCTCCAATGCACATCAAACTTCAGCACTTAAATCTCAGCTCCTTGTTTAAGTCTTGTCTGACATTTCGATATAAGAATTTAGAATCATTTATAGATGAACCATGATGCATCTACTAGAATGGTTTCATTTAAATCGCTATATCCATAACATTAAGAATGATGTTTACCTCTCTTTCTGGAGTTTGTTGTTGAAAGAAATCCTTCTTTTGGCTCAGACTCTTATTCCTGTATGTTCACTCCTACAGATTAGAGGTGGAAGCTGTAATGGAGCACACAAACAACACGGACACAAGGGCAAAAGACACACCTCCAGTGTTTTCTTCACTTCACAGACCTCTGGATATGGAGGACGGAGAGGCGGACGGAATGGAGATGGAGGCTGGAGCATCAGGAGGCGGTGGGGAGGAGTTTGTACCCATGGGT[C/T]AGTTGGAGAGCCTGGATCAGCCCAGTCTGTACCGTGATATCTGGAGTCTGCGCGCGTCTCTGGAGCAGTATGCTTCCTCAGACTTGAGCAGCAATGACAGAGACTCTACACGCAGCGATGCCGACAGCGTCTGCTCCGCAGGAGCCTCCAGAACAGGCATTCCCAGCTACCAGTCGCAGGACATCGATGATGATTTGGATGGGGAGCTGCCGTATGATGATATGATAAGGGATGTTGGACAGAGAAGAAACGGACGAGAGAGTCTGGACTCTGAAAGAGGCAGCGATGGAGAAACAAACAACCGCAAGCTCCTGCAGATGGACAGTGGCTACGCCTCGATTGAAGCTCCATGCAAAGCTCCAGAGGAACTCAGACTATTCGGAAGCGGCTCTGGAAAGACAGCGTCTGAGCGACGCCGCTTCTTCACCAATTCTGGCCGTAAAGGAACAGTTTGTGAGAGTTTTGAAGCGAGGCTTTTTAAAGAGGAGCTGGAGGATGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19916

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122394	Nonsense	312	631	3	3

Genomic Location (Zv9):

Chromosome 2 (position 59909017)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	58979446
GRCz11	2	59076737

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACAGTGGCTACGCCTCGATTGAAGCTCCATGCAAAGCTCCAGAGGAACTC[A/T]GACTATTCGGAAGCGGCTCTGGAAAGACAGCGTCTGAGCGACGCCGCTTC

Long Flanking Sequence:

CAAAAGACACACCTCCAGTGTTTTCTTCACTTCACAGACCTCTGGATATGGAGGACGGAGAGGCGGACGGAATGGAGATGGAGGCTGGAGCATCAGGAGGCGGTGGGGAGGAGTTTGTACCCATGGGTCAGTTGGAGAGCCTGGATCAGCCCAGTCTGTACCGTGATATCTGGAGTCTGCGCGCGTCTCTGGAGCAGTATGCTTCCTCAGACTTGAGCAGCAATGACAGAGACTCTACACGCAGCGATGCCGACAGCGTCTGCTCCGCAGGAGCCTCCAGAACAGGCATTCCCAGCTACCAGTCGCAGGACATCGATGATGATTTGGATGGGGAGCTGCCGTATGATGATATGATAAGGGATGTTGGACAGAGAAGAAACGGACGAGAGAGTCTGGACTCTGAAAGAGGCAGCGATGGAGAAACAAACAACCGCAAGCTCCTGCAGATGGACAGTGGCTACGCCTCGATTGAAGCTCCATGCAAAGCTCCAGAGGAACTC[A/T]GACTATTCGGAAGCGGCTCTGGAAAGACAGCGTCTGAGCGACGCCGCTTCTTCACCAATTCTGGCCGTAAAGGAACAGTTTGTGAGAGTTTTGAAGCGAGGCTTTTTAAAGAGGAGCTGGAGGATGAGGCAAGTTTGGAGCCAGAGCTTCCAAAGAGCCAAGAGACACAACCGACGACCAAACCTAGGCTACGATTCCGCCGCCGAGACTACAGCATCGATGAGAAGACGGAGGCGCTGTTTAATGAATTTCTAAGACATGATCCCCAGTTTGACCAACAGGGTTCACCCTCATTGCGACACCGGCACCGGTCCCGAATTCATCTCCGAAAGCAGTGGCAGCGCAGCAAACAGTACAGCGACCCAGGAGCCGCTCGATACTCACCGTCCCTAGAGCGCCAGCGCTGCTATCCGCTACGCAGAGGCGACAGTGCCAACTACCCACTGGATACACGATACCACAGTACCTTACCTCGCATCGCTAGTGCAGCAGATGAGGAG

Associated Phenotype:

Not determined